Allele Registry

Canonical Allele Identifier: PA162808

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122309

RCV000228291

RCV000857885

RCV002515905

RCV003078786

ClinVar Variation:

135452

2161864

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Leu383Phe	CA162806 NM_000553.6:c.1149G>T CA370920970 NM_000553.6:c.1149G>C